Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Chongfen, Chen"'
Autor:
Xiaona Wang, Jing Tao, Yidan Qiao, Shuying Luo, Zhenqin Zhao, Yinbo Gao, Jisheng Guo, Jinghui Kong, Chongfen Chen, Lili Ge, Bo Zhang, Pengbo Guo, Lei Liu, Yinsen Song
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Autism spectrum disorder (ASD) is an immensely challenging developmental disorder characterized by impaired social interaction, restricted/repetitive behavior, and anxiety. GABAergic dysfunction has been postulated to underlie these autistic symptoms
Externí odkaz:
https://doaj.org/article/505cc5fd686b400b855d0a24f2bfa6a1
Autor:
Pengbo Guo, Jinjin Liu, Lili Ge, Jinghui Kong, Lijun Zheng, Xuhui Chen, Yuqi Huo, Yinsen Song, Shuying Luo, Chongfen Chen
Publikováno v:
Virus Genes. 56:174-181
Genogroup II, genotype 4 noroviruses (GII.4 NoVs) are a leading cause of epidemic and sporadic acute non-bacterial gastroenteritis worldwide. In this study, we isolated a GII.4 NoV strain (designated 2015HN08) from a kid presenting with acute gastroe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9252712b371b7d391ca0f9140f9aedd3
https://doi.org/10.1007/s11262-019-01729-0
https://doi.org/10.1007/s11262-019-01729-0
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(9)
To detect variants of NF1 gene among thirteen patients with neurofibromatosis type 1.Genomic DNA was extracted from peripheral blood samples of the patients. High-throughput sequencing was employed to detect potential variants of the NF1 and NF2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a55a1b5fb2090c7f5bcaeab6429cda40
https://pubmed.ncbi.nlm.nih.gov/34487523
https://pubmed.ncbi.nlm.nih.gov/34487523
Autor:
Jiwen Cheng, Zhenjian Zhuo, Jing He, Lili Ge, Jiao Zhang, Li Yuan, Jinhong Zhu, Xianwei Zhang, Rui-Xi Hua, Chongfen Chen, Huimin Xia, Jing Liu, Haixia Zhou
Publikováno v:
Journal of Cellular and Molecular Medicine
Neuroblastoma ranks the most common seen solid tumour in childhood. Overexpression of LIN28A gene has been linked to the development of multiple human malignancies, but the relationship between LIN28A single nucleotide polymorphisms (SNPs) and neurob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06d2d714b1f871a3932aa242e6cae471
https://doi.org/10.1111/jcmm.14827
https://doi.org/10.1111/jcmm.14827
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(4)
To explore the clinical characteristics and genetic variants in a child with tyrosine hydroxylase-deficient infantile Parkinsonism with motor delay.Clinical feature of the patient was summarized. Genomic DNA was extracted from peripheral blood sample
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e6050dd536d42c052fdf0b7774bde39
https://pubmed.ncbi.nlm.nih.gov/32219836
https://pubmed.ncbi.nlm.nih.gov/32219836
Autor:
Pengbo Guo, Yinsen Song, Chongfen Chen, Shuying Luo, Lei Liu, Yidan Qiao, Zhenqin Zhao, Lili Ge, Jisheng Guo, Jinghui Kong, Yinbo Gao, Xiaona Wang, Bo Zhang, Jing Tao
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Frontiers in Neurology
Frontiers in Neurology
Autism spectrum disorder (ASD) is an immensely challenging developmental disorder characterized by impaired social interaction, restricted/repetitive behavior, and anxiety. GABAergic dysfunction has been postulated to underlie these autistic symptoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3043892c878aabe6803917dc73ef3795
https://www.frontiersin.org/article/10.3389/fneur.2018.01052/full
https://www.frontiersin.org/article/10.3389/fneur.2018.01052/full
Autor:
Shuying Luo, Lei Liu, Lili Ge, Chongfen Chen, Jingui Kong, Yinsen Song, Pengbo Guo, Yinghui Zhang, Bo Zhang
Publikováno v:
NeuroQuantology. 16
Cerebral palsy is a group of permanent limb posture and movement abnormalities caused by certain injuries to fetal or neonatal brain before its growth and development is completed. It is reported abroad that the incidence of cerebral palsy in live bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78599391f486dd31ac863853c63e0e60
https://doi.org/10.14704/nq.2018.16.6.1587
https://doi.org/10.14704/nq.2018.16.6.1587
Autor:
Chongfen Chen, Yinsen Song, Yinghui Zhang, Jingui Kong, Shuying Luo, Pengbo Guo, Lei Liu, Lili Ge, Bo Zhang
Publikováno v:
NeuroQuantology. 16
To explore the clinical features, diagnosis, and treatment of Wernicke’s encephalopathy (WE) in children and raise awareness of the disease. Summarize the clinical manifestations, diagnosis, and treatment characteristics of a WE case in a child pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a0d9c3717f6a802d5e65af04bef767f
https://doi.org/10.14704/nq.2018.16.5.1356
https://doi.org/10.14704/nq.2018.16.5.1356
Publikováno v:
Biochemical and biophysical research communications. 431(3)
Various physiological processes and behaviors show a circadian rhythm of approximately 24 h, which is crucial in coordinating internal metabolic processes and environmental signals. Post-translational modifications play an important role in regulatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84eb57dd3c2bb6ed82d299516bbfa3b3
https://pubmed.ncbi.nlm.nih.gov/23337503
https://pubmed.ncbi.nlm.nih.gov/23337503
Autor:
Ge, Lili, Chen, Xuhui, Liu, Jinjin, Zheng, Lijun, Chen, Chongfen, Luo, Shuying, Guo, Pengbo, Kong, Jinghui, Song, Yinsen, Huo, Yuqi
Publikováno v:
Virus Genes; Apr2020, Vol. 56 Issue 2, p174-181, 8p